{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "If the C-arm is manually moved in the longitudinal direction to a fully extended position, the system's safety stop mechanism may be activated. As a result, the C-arm stops the movement and can drop up to 20 mm (0.8 ). Under certain circumstances, the cover of the detector or collimator can touch and possibly injure the patient due to the C-arm drop. This could lead to a situation in which it is necessary to stop the clinical treatment or continue the treatment on an alternative system.",
      "address_2": "",
      "product_quantity": "39",
      "code_info": "164033  164071  164034  164095  164057  164055  164054  164080  164072  164088  164048  164094  164068  164019  164013  164073  164027  164026  164025  164060  164083  164021  164066  164075  164084  164086  164074  164098  164028  164053  164063  164064  164024  164049  164022  164018  164100  164097  164011",
      "center_classification_date": "20180622",
      "distribution_pattern": "Healthcare facilities in AL, CA, CO, FL, IL, KY, MA, MI, MN, MS, NE, NJ, NY, OH, TN, TX, UT, and VA. Foreign distribution to Australia, Austria, Belgium, Denmark, France, Germany, Italy, Japan, Kuwait, Netherlands, Norway, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, and United Kingdom.",
      "state": "PA",
      "product_description": "ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000",
      "report_date": "20180704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-2283-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80272",
      "termination_date": "20200318",
      "more_code_info": "",
      "recall_initiation_date": "20180501",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Completed"
    }
  ]
}